Au/Fe2O3 catalyst materials, method for the production thereof and their use

ABSTRACT

The invention relates to an Au/Fe 2 O 3  catalyst comprised of a particle-shaped, co-catalytically active Fe 2 O 3  supporting material with metallic Au clusters deposited thereupon which have a diameter of less than 4.5 nm. The catalyst materials can be obtained by: a) reacting a water-soluble Fe(III) salt in an aqueous medium with a base; b) impregnating the hydroxide gel which is formed thereby and which is still moist with a solution of a water-soluble Au compound in order to deposit complexed Au clusters on the surface of the hydroxide gel; c) removing water from the suspension of the reaction product formed thereby; d) subjecting the dried reaction product to a calcination at temperatures ranging from 350 and 700° C. The inventive catalyst material is especially suited for selective low-temperature CO oxidation in reformate hydrogen which is used as combustible gas for polymer electrolyte membrane (PEM) fuel cells.

The present invention relates to Au/Fe₂O₃ catalyst materials made from a particulate, co-catalytically active Fe₂O₃ support material with metallic Au clusters deposited thereon which have a diameter of less than 4.5 nm, various processes for their production and their use, particularly for selective low-temperature CO oxidation in reformate hydrogen.

The CO content in reformate hydrogen from a hydrocarbon reformer is about 5,000 ppm or over 10,000 ppm to 20,000 ppm immediately downstream of a methanol reformer. When using such a reformate hydrogen as combustible gas in polymer-electrolyte-membrane (PEM) fuel cells, this CO must be reduced almost completely, that is to about 30 ppm maximum not to poison the Pt/Ru—C anodes of the PEM fuel cell conventionally used. To reduce the CO content in reformate hydrogen, there are several chemical engineering concepts, of which selective CO oxidation is currently preferred for mobile applications and small stationary plants for reasons relating to cost and selectivity, but also because of the comparatively high space-time yield.

This oxidative CO removal is traditionally carried out in a multi-stage reactor by means of known high-temperature catalysts, for example Pt/Al₂O₃, at 200° C. The control of such a reactor system for continuously guaranteeing a residual CO content of about 30 ppm at different load states of the fuel cell is however extremely expensive and complicated. One of the main reasons for this, which occurs particularly during transfer to weak loads with larger residence times associated therewith, is the retro-shift reaction (3) competing with the reaction equations (1) and (2) shown below, and which has to be repressed, for example by rapid increase of oxygen supply while reducing the required selectivity.

CO+½O₂→CO₂  (1)

H₂+½O₂→H₂O  (2)

CO₂+H₂→CO+H₂O  (3)

Catalyst materials have been developed, in which the Pt has been replaced by Ru or a different Pt group metal, and which have the same activity and selectivity as the traditional Pt/Al₂O₃ catalyst material in the temperature range from 120 to 150° C. at comparable noble metal content.

For reasons relating to kinetics and process technology, it is advantageous to allow CO coarse cleaning to proceed in the temperature range from 190 to 230° C. in a fixed bed reactor operating as isothermally as possible and filled with traditional Pt/Al₂O₃ pellets. The second or last cleaning stage (CO fine cleaning at CO starting contents of 1,000 to 2,000 ppm) is then carried out at considerably lower temperatures, for example at 120° C., using the above-mentioned catalyst materials.

Furthermore, it has been proposed to shift the CO fine cleaning to the working region of the PEM fuel cell, that is at temperatures up to 80° C., but for which a low-temperature CO oxidation catalyst is required.

It is known that metal oxide-supported Au catalysts show high catalytic activity during low-temperature oxidation of CO even in reducing atmosphere. Hence, it can be seen from Journal of Catalysis 168 (1997) 125-127, that an Au catalyst (Au/MnO_(x) catalyst) supported on manganese oxides may be used for selective oxidation of CO in hydrogen. The production of the Au/MnO_(x) catalyst is effected by coprecipitation of an aqueous solution of tetrachloroauric acid and manganese nitrate with an aqueous lithium carbonate solution, drying and calcining of the coprecipitate in air at 300° C. The calcined sample thus consists mainly of metallic gold particles and MnCO₃. After measuring the catalytic activity for CO oxidation in hydrogen for one day, decomposition of MnCO₃ occurred with formation of crystalline manganese oxides, MnO, Mn₃O₄ and Mn₂O₃. In addition, there was sintering of the gold particles, wherein an average particle diameter of 2.8 nm was obtained. However, the CO conversion rate of such a catalyst material is relatively low and not satisfactory for practical application.

Applied Catalysis A: General 134 (1996) 275-283 reports on the low-temperature water gas shift reaction on Au/Fe₂O₃ catalysts produced by coprecipitation. It can be seen from this that a higher catalytic activity results with smaller gold particle diameter. The CO conversion rate of an Au/Fe₂O₃ catalyst material produced by coprecipitation is however likewise not satisfactory.

German Offenlegungsschrift 4 238 640 describes Au/Fe₂O₃ catalysts for hydrogenating CO and CO₂, which likewise are produced by mixed precipitation of a gold compound and an iron salt.

The object of the present invention is to provide an Au/Fe₂O₃ catalyst material having increased activity and selectivity, particularly for low-temperature CO oxidation, and adequate long-term stability, and processes for its production.

This object is achieved by a catalyst material according to claims 1 and 3 and processes according to claims 7, 8 and 9. Advantageous or preferred embodiments of the inventive object are given in the sub-claims.

Accordingly, the object of the invention is an Au/Fe₂O₃ catalyst material made from a particulate, co-catalytically active Fe₂O₃ support material with metallic Au clusters deposited thereon which have a diameter of less than 4.5 nm, which can be obtained by

a) reacting a water-soluble Fe(III) salt in an aqueous medium with a base,

b) impregnating the still moist hydroxide gel thus formed with a solution of a water-soluble Au compound to deposit complexed Au clusters on the surface of the hydroxide gel,

c) removing water from the suspension of the reaction product thus formed, and

d) subjecting the dried reaction product to calcining at temperatures between 350 and 700° C.

According to a preferred embodiment, this catalyst material also contains at least one Fe₂O₃ sinter inhibitor selected from Al₂O₃, Cr₂O₃ and MgO.

The object of the invention is also an Au/Fe₂O₃ catalyst material made from a particulate, co-catalytically active Fe2O₃ support material containing at least one Fe₂O₃ sinter inhibitor selected from Al₂O₃, Cr₂O₃ and MgO and with metallic Au clusters deposited thereon which have a diameter of less than 4.5 nm, which can be obtained by:

i) simultaneously reacting a water-soluble Fe(III) salt, at least one water-soluble salt of Al, Cr, Mg and a water-soluble Au compound in an aqueous medium with a base,

ii) removing water from the suspension of the reaction product thus formed, and

iii) subjecting the dried reaction product to calcining at temperatures between 350 and 700° C.

The catalyst material of the invention preferably contains 2-8 wt. % Au, since the best results are obtained with such a gold deposit.

Furthermore, it is desirable that the catalyst material of the invention has as high as possible specific surface area, preferably of at least 50 m²/g according to the BET method. Furthermore, the Au clusters in the catalyst material of the invention have as high as possible a degree of dispersion, so that the Au clusters preferably have a diameter of less than 4 nm, also preferably of 1-3 nm.

A high specific oxide surface area and a high degree of dispersion for the Au clusters are particularly advantageous as regards kinetic points of view, since the step determining the reaction rate during CO oxidation takes place on the gold-iron oxide boundary. The degree of dispersion of the gold is therefore very important with regard to the CO conversion rate for the same Au deposit.

Regarding the CO selectivity of the catalyst materials of the invention, it has been shown that the selectivity increases for a temperature reduction from, for example 80 to 20° C. This can be explained in that at lower temperatures CO is generally absorbed more strongly than H₂. However, the rate of CO oxidation also drops with a reduction in temperature.

The Au/Fe₂O₃ catalyst materials of the invention show an excellent long-term stability. For example the catalyst material of the invention shows no change on one-week long storage under real reformer gas atmosphere with traces of oxygen at 80° C. The presence of 0.3 to 1% oxygen in the reformer gas suppresses the reduction of Fe₂O₃ to form Fe₃O₄ and the formation of FeCO₃.

Investigations have shown that the CO oxidation activity of the Au/Fe₂O₃ catalyst of the invention is higher by at least a factor 50, for comparable gold particle size between 2.5 and 4.5 nm, than for the known Au/MnO_(x) catalyst (see also examples).

In one embodiment of the process of the invention, the catalyst material is not produced by coprecipitation, but a reaction of a water-soluble Fe(III) salt is initially effected in an aqueous medium with a base with formation of an iron oxide precursor, namely an iron hydroxide gel, wherein in a second step immediately thereafter, the still moist hydroxide gel is impregnated with a solution of a water-soluble Au compound to deposit complexed Au clusters on the surface of the hydroxide gel in the finest distribution. After removing water, the dried reaction product is then subjected to calcining at temperatures between 350 and 700° C.

The production process of the invention permits a better, that is independent, control of the optimised pre-structures of the two reaction components. Hence, for example during the first precipitation by suitable temperature control via the grain growth rate of Fe(O) (OH)_(x) precursor matrix, the content of surface hydroxyl groups and the water adsorbates may be adjusted not only in the hydroxide gel itself, but in the end in the pre-dried end product. Following on from that there is deposition using the dissociated, anionic Au complex, for example in the form of an [Au(Cl)_(4-z)(OH)_(z)]⁻ complex when using tetrachloroauric acid as the water-soluble Au compound.

According to the invention, much smaller Au clusters having an average diameter of less than 4.5 nm, in particular between 1 and 3 nm, can be fixed on the Fe₂O₃ support material by this process of sequential precipitation than by the known coprecipitation, in which at best gold islands having a diameter of about 4.5 nm are obtained. The increased degree of dispersion of the gold achieved according to the invention facilitates a CO conversion increase per gram of gold by a factor of 3 to 5.

According to a modified embodiment of the process of the invention described above, the first step of conversion of a water-soluble Fe(III) salt takes place in the presence of at least one water-soluble salt of Al, Cr or Mg in order to obtain a catalyst material which also contains at least one Fe₂O₃ sinter inhibitor selected from Al₂O₃, Cr₂O₃ and MgO.

In a third embodiment, the Au/Fe₂O₃ catalyst material containing at least one Fe₂O₃ sinter inhibitor selected from Al₂O₃, Cr₂O₃ and MgO is produced according to a process, which comprises the following steps:

i) simultaneously reacting a water-soluble Fe(III) salt, at least one water-soluble salt of Al, Cr, Mg and a water-soluble Au compound in an aqueous medium with a base,

ii) removing water from the suspension of the reaction product thus formed, and

iii) subjecting the dried reaction product to calcining at temperatures between 350 and 700° C.

The effect of the oxides Al₂O₃, Cr₂O₃ or MgO, which have grown into the Fe₂O₃ crystal matrix and are formed after calcining, consists in preventing the slow sintering of haematite (α-Fe₂O₃) or magnetite (Fe₃O₄) substrate and the migration and coagulation of the gold clusters during use of the catalyst material. The use of MgO as “spacer” is thus particularly preferred according to the invention, since the two Fe and Mg oxide precursors thus do not exist separately from one another during the production of the catalyst material, but as an Mg—Fe compound, for example as Mg₆Fe₂CO₃(OH)₁₆.4H₂O (pyroaurite), together with amorphous Fe₂O₃. A very homogeneous mixture of the two oxides is thus achieved during calcining and the “spacer” effect of MgO on the Fe₂O₃ or on the MgFe₂O₄ precursor is maximised. At the same time, the mobility of the Au particles on the oxidic surface is thus restricted even during the heating time of the calcining step, as a result of which very small gold clusters are preserved. Furthermore, it may be assumed that the amorphous MgO increases the catalytic synergistic effect of molecular oxygen promotion or cleavage on the Fe₂O₃ surface. Finally, the carbon dioxide, which escapes as gas during calcining at about 350-400° C., effects the formation of a secondary gas pore structure, which is desirable in the subsequent formation of catalyst pellets or in the production of a pressed catalyst insert sheet.

In the process of the invention, the precipitation and impregnation steps are preferably carried out at temperatures of 40-95° C., also preferably at 60-85° C.

The pH value in the precipitation and impregnation steps is preferably 6-10, also preferably 7-9.

Suitable bases are known metal hydroxides and/or metal carbonates, wherein preferably NaOH and/or Na₂CO₃, in particular Na₂CO₃, are used.

The water-soluble salts of Al, Cr or Mg are preferably used in a proportion of 0.1-3.0 moles, also preferably 0.1-1.0 mole, and still further preferably 0.1-0.5 mole, per mole of Fe.

Suitable water-soluble gold compounds are, for example tetrachloroauric acid or tetranitratoauric acid, wherein tetrachloroauric acid is particularly preferred. Fe(NO₃)₃ is preferably used as the water-soluble Fe(III) salt, and may alternatively contain water of crystallisation.

Calcining is effected suitably at temperatures between 350 and 700° C., preferably between 350 and 500° C., also preferably between 350 and 400° C., wherein the last-mentioned temperature range is used particularly when none of the sinter inhibitors mentioned are used.

The catalyst material of the invention is suitable, for example for selective CO oxidation in reformate hydrogen, for methanisation, for CO conversion or for oxidative removal of CO and of hydrocarbons from air. The use for selective low-temperature CO oxidation in reformate hydrogen for PEM fuel cells is particularly preferred. The catalyst material of the invention may thus be processed to form pellets according to traditional processes or be pressed to form a catalyst insert sheet.

The following examples illustrate the invention.

COMPARATIVE EXAMPLE 1

According to the process described in Applied Catalysis A: General 134 (1996) 275-283, 50.5 g of Fe(NO₃)₃.9H₂O and 1.12 g of HAuCl₄.3H₂O are dissolved in 125 ml of deionised water and, together with a 1 M Na₂CO₃ solution, added dropwise to 150 ml of water pre-heated at 80° C. with intensive stirring. The pH value is thus adjusted to 7.9 to 8.1 and the temperature is kept constant at 80° C. After about 30 minutes precipitation is completed and stirring is continued for about a further 45 minutes. After cooling, the suspension is filtered and washed several times using warm water until free of chloride (checking by AgNO₃ test). The filter cake is then dried overnight at 80° C. and then ground.

The X-ray diffraction pattern shows an amorphous structure related to α-Fe₂O₃ or γ-Fe₂O₃. The BET surface area is about 170 m²/g, wherein the average pore diameters on the one hand are below 0.8 nm and on the other hand fairly close at 1.8 nm. After calcining for 30 minutes at 400° C., the BET surface area is about 54 m²/g. X-ray diffraction shows a semi-crystalline α-Fe₂O₃ phase (haematite). The gold particle diameter may thus be estimated at 4.5 nm by means of the Scherrer equation.

The sample contains 3.2 wt. % of Au (60% degree of deposition), based on the anhydrous oxide composition.

The kinetic CO conversion measurement at 80° C. in a fixed bed micro-reactor under differential flow conditions (gas atmosphere: 1% CO, 1% O₂, 75% H₂, remainder N₂) produces a CO conversion rate of 1.14.10⁻³ moles/s.g(Au). As the comparison with an Au/MnO_(x) catalyst (Reference 1) in the following table known from Journal of Catalysis 168 (1997) 125-127 shows, the CO conversion rate for traditional Au/Fe₂O₃ catalyst material proves indeed to be greater by at least a factor 25, but is not yet satisfactory.

EXAMPLE 1

The process of comparative example 1 is repeated, with the exception that the precipitation is effected in the absence of tetrachloroauric acid. After precipitation, the suspension is cooled to 60° C. with stirring, and 30 ml of 0.1 molar tetrachloroauric acid solution are added dropwise in the course of 5 minutes at pH 8.0, buffered using Na₂CO₃ solution and then stirred for a further 30 minutes. The further working up is effected according to comparative example 1.

The BET surface area of the completely amorphous powder after drying is about 280 m²/g. The corresponding catalyst data after calcining (likewise 30 minutes at 400° C.) are given in the following table. As can be seen, the activity (rate of CO oxidation per gram of gold) of the catalyst material of the invention is clearly increased compared to Reference 1 and comparative example 1.

EXAMPLE 2

35.9 g of Fe(NO₃)₃.9H₂O, 22.8 g of Mg(NO₃)₂.6H₂O and 1.59 g of HAuCl₄.3H₂O are dissolved in 180 ml of water and this solution, together with 1 M Na₂CO₃ solution, is added dropwise into a flashback chamber (400 ml) in the same manner as described in comparative example 1 at 85 to 90° C. and pH 7. In accordance with the further steps according to comparative example 1, a light brown powder is obtained after drying having a very amorphous basic structure, in which proportionally pyroaurite (Mg₆Fe₂CO₃(OH)₁₆.4H₂O) can be identified. Analysis of the decomposition precursor in the TGA apparatus supports the presence of this compound. After calcining (30 minutes at 400° C.), in spite of the excess of Fe₂O₃, the powder remains amorphous radiographically, as also confirmed by the high specific (BET) surface area of 190 m²/g in the last line of the following table. The activity of the catalyst powder thus produced is comparable with the activity of the catalyst from Example 1 produced by the impregnation method.

TABLE Speci- Phases Au Diameter fic accor- con- of Au surface ding to Rate^(a) tent Par- area X-ray mmoles Wt. ticles (BET) diffrac- CO/s.g- System % nm m²/g tion (Au) Refe- Au/MnO_(x) 5 2.8 Not Mn₃O₄ + 0.05^(b) rence measured remain- 1 der MnCO₃ Compa- Au/Fe₂O₃ 3.2 4.5 54 α-Fe₂O₃ 1.14 rative exam- ple 1 Exam- Au/Fe₂O₃ 2.3 2.5 60 α-Fe₂O₃ 5.7 ple 1 Exam- Au/Fe₂O₃ 2.3 <4 190 Amor- 4.6 ple 2 with MgO phous ^(a)at 80° C. after 2 hours in 1% CO, 1% O₂, 75% H₂, remainder N₂ ^(b)98% H₂, no N₂ 

What is claimed is:
 1. Process for producing an Au/Fe₂O₃ catalyst material made from a particulate, co-catalytically active Fe₂O₃ support material having metallic Au clusters deposited on the Fe₂O₃ support material, said clusters having a diameter of less than 4.5 nm, said method comprising the following steps: a) reacting a water-soluble Fe(III) salt in an aqueous medium with a base, thereby forming a moist hydroxide gel; b) impregnating the moist hydroxide gel with a solution of a water-soluble Au compound to deposit complexed Au clusters on the surface of the hydroxide gel, thereby forming a suspension of reaction products; c) removing water from the suspension of reaction products, thereby forming a dried reaction product; and d) subjecting the dried reaction product to calcining at temperatures between 350 and 700° C.
 2. Process for producing an Au/Fe₂O₃ catalyst material according to claim 1, wherein said catalyst contains furthermore at least one Fe₂O₃ sinter inhibitor selected from Al₂O₃, Cr₂O₃ and MgO, and which can be obtained by adding at least one water-soluble salt of Al, Cr or Mg in step a).
 3. Process for producing an Au/Fe₂O₃ catalyst material according to claim 1, further comprising the steps of: adding at least one water-soluble salt of Al, Cr or Mg in step a).
 4. Process for producing an Au/Fe₂O₃ catalyst material according to claim 1, wherein said catalyst material contains 2-8 wt. % Au.
 5. Process for producing an Au/Fe₂O₃ catalyst material according to claim 1, having a specific BET surface area of at least about 50 m²/g.
 6. Process for producing an Au/Fe₂O₃ catalyst material according to claim 1, wherein the Au clusters have a diameter of less than 4 nm.
 7. Catalyst material according to claim 6, wherein the Au clusters have a diameter of 1-3 nm.
 8. Process according to claim 1, wherein steps a)and b) are carried out at temperatures of 40-95° C.
 9. Process according to claim 1, wherein steps a) and b) are carried out at a pH value of 6-10.
 10. Process according to claim 1, wherein metal hydroxides and/or metal carbonates are used as the base in step a).
 11. Process according to claims 3, wherein the water soluble salt of Al, Cr or Mg is used in step a) in a proportion of 0.1-3.0 moles per mole Fe.
 12. Process according to claims 1, wherein tetrachloroauric acid or tetranitratoauric acid is used as the water-soluble Au compound.
 13. Process according to claim 1, wherein Fe(NO₃)₃ is used as the Fe(III) salt.
 14. Process according to claim 8, wherein steps a) and b) are carried out at temperatures of 60-85° C.
 15. Process according to claim 9, wherein steps a) and b) are carried out at a pH value of 7-9.
 16. Process according to claim 10, wherein NaOH and/or Na₂CO₃ are used as the base in step a).
 17. Process according to claim 11, wherein the water soluble salt of Al, Cr or Mg is used in step a) in a proportion of 0.1-1.0 mole per mole Fe.
 18. Process according to claim 11, wherein the water soluble salt of Al, Cr or Mg is used in step a) in a proportion of 0.1-0.5 mole per mole Fe. 